Keil Philip M, Hadlington Terrance J
Fakultät für Chemie, Technische Universität München, Lichtenbergstraße 4, Garching 85747, Germany.
Chem Commun (Camb). 2022 Mar 1;58(18):3011-3014. doi: 10.1039/d2cc00422d.
We describe facile synthetic methods for accessing linear cationic tetrylene nickel(0) complexes [DippE·Ni(PPh)] (E = Ge (4) and Sn (5); Dipp = [(iPrSi)(Dipp)N]), which feature donor-acceptor E-Ni triple bonds. These species are readily accessed in a one-pot protocol, combining the bulky halo-tetrylenes DippECl (E = Ge (1) and Sn (2)), Ni(cod), PPh, and Na[BAr]. Given the diamagnetic nature of 4 and 5, they each contain a formal zero-valent Ni centre, making the E-M triple bonds in these complexes unique compared to previously reported metal tetrylidyne complexes, which typically feature covalent/ionic bonding. In-depth computational analyses of these species further support triple bond character in their E-Ni interactions.
我们描述了用于合成线性阳离子四价镍(0)配合物[DippE·Ni(PPh)](E = Ge (4) 和 Sn (5);Dipp = [(iPrSi)(Dipp)N])的简便合成方法,这些配合物具有给体-受体E-Ni三键。通过一锅法,将体积较大的卤代四价物DippECl(E = Ge (1) 和 Sn (2))、Ni(cod)、PPh和Na[BAr] 相结合,可轻松得到这些物种。鉴于4和5的抗磁性,它们各自包含一个形式上的零价Ni中心,这使得这些配合物中的E-M三键与先前报道的金属次四价物配合物相比具有独特性,后者通常具有共价/离子键。对这些物种的深入计算分析进一步支持了它们E-Ni相互作用中的三键特征。